ライフサイエンスコーパス: adhesive property

1 eatures typically exhibit intriguing surface adhesive properties.

2 d a distinct class of membrane proteins with adhesive properties.

3 ) were isolated based on their intercellular adhesive properties.

4 ovary (CHO) cells and examined the relative adhesive properties.

5 first direct evidence that fertilin beta has adhesive properties.

6 rticles will exhibit interesting anisotropic adhesive properties.

7 e notion that myelin TJs exhibit significant adhesive properties.

8 d choline-binding protein displaying various adhesive properties.

9 d simultaneously mapped their mechanical and adhesive properties.

10 offer independent control over physical and adhesive properties.

11 lgi apparatus, respectively, activates their adhesive properties.

12 aminin in vitro, suggesting that MTP possess adhesive properties.

13 asion and metastasis by reducing cancer cell adhesive properties.

14 ng signaling pathways or modulating cellular adhesive properties.

15 osylation of MSP1a significantly reduced its adhesive properties.

16 ies, and the other (integrins) with strongly adhesive properties.

17 y each receptor that underpin their specific adhesive properties.

18 These cell clusters also have differential adhesive properties: adherens junction components are up

19 further demonstrate that regulation of cell adhesive properties and cell morphology may underlie the

20 Yersinia pestis the autotransporter YapE has adhesive properties and contributes to disease in the mo

21 odify axon behavior in vitro by altering the adhesive properties and cytoskeleton of olfactory recept

22 Amniotic membrane has anti-adhesive properties and is felt to promote epithelializa

23 roduct(s) of fibrinogen cleavage have strong adhesive properties and may be similar to fibrin.

24 ydrogels were optimized first regarding cell adhesive properties and mechanical properties to best su

25 Moreover this action is dependent on the adhesive properties and the C terminus of Cx43 but not t

26 of developing DRG neurons may modulate their adhesive properties and thereby support axonal developme

27 results in substantial enhancement of OPN's adhesive properties, and because VPF/VEGF promotes incre

28 These processes determine the shape, adhesive properties, and movement of cells, and the Rho

29 (selectins or selectin ligands) with weakly adhesive properties, and the other (integrins) with stro

30 role in hemostasis and thrombosis, platelet adhesive properties are central to a variety of pathophy

31 It also allows for the variation of these adhesive properties, as would occur in the presence of a

32 that can be used repeatedly with peeling and adhesive properties better than the natural gecko foot.

33 nal consequences of mismatched stiffness and adhesive properties between neighboring normal cells on

34 ntified the impact of polysialylation on the adhesive properties both of membrane-bound neural cell a

35 ro active agent release profile and in vitro adhesive properties, both to oral mucosa and to teeth su

36 ells not only positively influenced cellular adhesive properties but also reversed the transformed ph

37 on complex and the consequent acquisition of adhesive properties by the cells.

38 YapE also demonstrates adhesive properties capable of mediating interactions wi

39 Regulation of the adhesive properties during erythroid differentiation may

40 ed enzyme, the recombinant proteins retained adhesive properties equal to the natural T. vaginalis AP

41 racteristics, e.g. their density, fragility, adhesive properties, etc.

42 receptor complexes rapidly alters the cell's adhesive properties facilitating high avidity cell-ligan

43 's gliding speed and its ability to modulate adhesive properties for successful exit from the inocula

44 ytohesin 1 (CYTH1) as a critical mediator of adhesive properties in primary human cord blood-derived

45 from vitelline membrane, and that this anti-adhesive property is important to prevent precocious adh

46 antigen I/II family polypeptide that confers adhesive properties linked to pathogenesis in GBS.

47 Moreover, the adhesive property occurred in both homotypic with Cx50 e

48 Mimicking the non-adhesive properties of a glycocalyx provides a potential

49 ulation modulates alpha IIb beta 3-dependent adhesive properties of a human erythroleukemic (HEL) cel

50 ereby thrombin cleavage of HC1 regulates the adhesive properties of an inflammatory HA matrix.

51 Thus, tRA alters the adhesive properties of APL cells by inducing the express

52 between tRA-induced differentiation and the adhesive properties of APL cells.

53 , produced by Bacillus thuringiensis, on the adhesive properties of BBMVs were investigated.

54 2 enhanced the chemotaxis, chemoinvasion and adhesive properties of breast cancer cells; parameters t

55 The mechanical and adhesive properties of cancer cells significantly change

56 ort-term reaggregation assays to compare the adhesive properties of cells derived from midbrain and a

57 Adhesive properties of cells undergoing morphogenetic re

58 pe I transmembrane mucin that can affect the adhesive properties of cells, contains a large extracell

59 sting one function of Dll here is to control adhesive properties of cells.

60 residue known for its essential role in the adhesive properties of classic cadherins.

61 We also compared the hydrophobic and adhesive properties of DeltabclA and wild-type spores.

62 In contrast, TGF-beta1 has no effect on the adhesive properties of DMEC from psoriatic plaques, and

63 udy of the substrate and oxidation-dependent adhesive properties of dopa.

64 has previously been used to demonstrate the adhesive properties of E-cadherin.

65 ortant differences regarding the nonspecific adhesive properties of each layer.

66 ating the proper migration and/or changes in adhesive properties of early embryonic cells.

67 The intrinsic contractile, migratory, and adhesive properties of endothelial cells are central det

68 important role in mediating the cell-matrix adhesive properties of epithelial cells.

69 hanism whereby circulating fibrinogen alters adhesive properties of fibrin clots may have important i

70 f the multilayer formation, the physical and adhesive properties of fibrinogen matrices prepared from

71 To examine the adhesive properties of full-length PECAM-1 in a native l

72 To obtain information on the adhesive properties of GalCer bilayers, we incorporated

73 migration, raising the possibility that the adhesive properties of gap junctions may have an importa

74 Waals mechanism implies that the remarkable adhesive properties of gecko setae are merely a result o

75 In this study, we set out to investigate the adhesive properties of H7 and H6 flagella.

76 apid, temporally progressive decrease in the adhesive properties of hepatocytes exposed to such serum

77 mains which might contribute to the specific adhesive properties of IEs.

78 SFA measurements and are used to extract the adhesive properties of individual amino acids within the

79 Here we have studied the adhesive properties of integrin alphaLbeta2 containing m

80 may modulate the molecular interactions and adhesive properties of its ectodomain.

81 ity of the molecule and demonstrate that the adhesive properties of McaP do not require its lipolytic

82 stages of erythroid differentiation, but the adhesive properties of more primitive murine erythroid p

83 tly with glycosaminoglycans, we examined the adhesive properties of multiple monovalent and multivale

84 The adhesive properties of Mytilus edulis foot proteins mfp-

85 nisms for this trait may perhaps be the anti-adhesive properties of NDM or its potential effect on in

86 s may be caused by abnormalities in the cell adhesive properties of neuroepithelial cells and suggest

87 el Toro et al. (2017) show that changing the adhesive properties of neurons in the normally lissencep

88 The growth-inhibitory and anti-adhesive properties of NG2 may limit the lateral extensi

89 the hindbrain, this is a result of different adhesive properties of odd- and even-numbered segments (

90 BC) to C. albicans adhesion and assessed the adhesive properties of other NT-Als3 features in the abs

91 The finding that the adhesive properties of PECAM-1 are regulatable suggests

92 pxB leads to down-regulation of the multiple adhesive properties of pneumococcus which, in turn, may

93 effect of alpha-actinin-4 deficiency on the adhesive properties of podocytes in vivo and in a cell c

94 of Yersinia pestis consists of fimbriae with adhesive properties of potential importance for the path

95 is study examined the antibacterial and anti-adhesive properties of pure plant extracts (PPEs) of gre

96 f keratinocytes, and the preservation of the adhesive properties of stratified epithelium.

97 GF, produced by the ectoderm, influences the adhesive properties of the adjacent mesoderm cells durin

98 discoideum motility with an emphasis on the adhesive properties of the cell-substratum contact.

99 V-histidine kinase, LovK, that regulates the adhesive properties of the cell.

100 This lock may be achieved by a change in the adhesive properties of the cells: cadherin-based adhesio

101 sociated with reduced IL-1 receptor-mediated adhesive properties of the endothelium and is protective

102 determine the effect of Psgl-1 deficiency on adhesive properties of the endothelium and on leukocyte

103 cribe a systematic investigation of the cell-adhesive properties of the extracellular region of RPTPm

104 of the intracellular C terminus enhances the adhesive properties of the extracellular surface of AQP0

105 The mechanical and adhesive properties of the fuzzy coat are modulated by e

106 a or Cys435Ala substitution of GPIIIa on the adhesive properties of the GPIIb-IIIa complex.

107 ically, we address the impact of t-RA on the adhesive properties of the human mature B and T cell lin

108 To study the adhesive properties of the LFA-1 I domain, we stably exp

109 ecades, many scenarios based on the enhanced adhesive properties of the membrane of sickle red blood

110 initial mutation, and the proliferative and adhesive properties of the mutant cells, to obtain stati

111 This is likely due to abnormal adhesive properties of the mutant hepatocytes, which may

112 polysialic acid expression and influence the adhesive properties of the neural cell adhesion molecule

113 ss-linking may explain in part the increased adhesive properties of the Pro(33) variant of integrin b

114 zed the regulatory network of YloA-dependent adhesive properties of the probiotic B. subtilis natto (

115 ro and in vivo experiments indicate that the adhesive properties of the proteolipid protein, along wi

116 xpression, ordered spatial localization, and adhesive properties of the RGM-related family of membran

117 es stringent requirements for smoothness and adhesive properties of the surface, which most common su

118 quartz surfaces in an attempt to change the adhesive properties of the surfaces.

119 ephrin activation may in part be due to the adhesive properties of the tissue.

120 ibronectin type III domains that mediate the adhesive properties of this group of transmembrane prote

121 unique sulfated structures may modulate the adhesive properties of TN-R over the course of developme

122 rminal fragment can functionally restore the adhesive properties of Tractin.

123 llular activation signals that influence the adhesive properties of vascular cells that express this

124 required to maintain proper conformation and adhesive properties of VE-cadherin, do not influence the

125 subvirucidal concentrations, EB changes the adhesive properties of virions, causing aggregation at h

126 9.5 and is most likely a result of different adhesive properties of wild-type and mutant cells.

127 This role is mediated in part through the adhesive properties of Xcyr61 and its related ability to

128 Anti-adhesive property of extracts was evaluated in Caco-2 ce

129 In vitro, the anti-adhesive property of NDM was validated on epithelial cel

130 m by which Disabled-1 signaling controls the adhesive property of neurons to radial glia, thereby mai

131 developmentally regulated and modulates the adhesive property of the neural adhesion molecule, N-CAM

132 degradation of fibrin(ogen) and also confer adhesive properties on cells because Mac-1 and uPAR bind

133 que to determine the spatial distribution of adhesive properties on rolling cell surfaces.

134 Changes in adhesive properties on tumor endothelial subclones are a

135 onstrate that the H6 and H7 flagella possess adhesive properties, particularly the ability to bind mu

136 4beta1 and alpha5beta1 confer different cell adhesive properties, particularly with respect to focal

137 These are the smallest peptides with adhesive properties reported to date and show remarkable

138 At the leading edge, cells show altered adhesive properties such that they form ectopic contacts

139 Like YapV, YapK and YapJ demonstrated adhesive properties, suggesting that their previously re

140 ribute to regulating changes in cell surface adhesive properties that affect the propensity of cells

141 oordination of alterations in cell shape and adhesive properties that are mediated by cytoskeletal dy

142 is can provide T lymphocytes with motile and adhesive properties that are uniquely suited toward alte

143 glycoprotein displays both adhesive and anti-adhesive properties that contribute to the formation and

144 alized to the plasma membrane, Prmp displays adhesive properties that may be important for linking th

145 This gives rise to a spectrum of adhesive properties that strongly influences interaction

146 om the binding of bacteria with well-defined adhesive properties to blots of SDS-PAGE-separated parot

147 reatment of cells with 5T-Fuc impaired their adhesive properties to immobilized adhesion molecules an

148 sed that inhibition of apoptosis and altered adhesive properties to the bone marrow microenvironment

149 in-transfected cell lines showed significant adhesive properties under conditions where cells transfe

150 ce both Daudi and Jurkats do not alter their adhesive properties upon t-RA treatment.

151 in thrombus formation, we analyzed receptor adhesive properties using Chinese hamster ovary and huma

152 As with HIV-infected EC, adhesive properties were linked to the capacity of Vpu t

153 the Vpu gene, CD40 upregulation and BL-cell adhesive properties were lost, indicating an essential r

154 eries of oligopeptides with beta-forming and adhesive properties, were synthesized and analyzed for a